@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_head {
  this: np:hasAssertion dgn-np:NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_assertion;
    np:hasProvenance dgn-np:NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_provenance;
    np:hasPublicationInfo dgn-np:NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_assertion a np:Assertion .
  
  dgn-np:NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_provenance a np:Provenance .
  
  dgn-np:NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_assertion {
  miriam-gene:6532 a ncit:C16612 .
  
  lld:C0029421 a ncit:C7057 .
  
  dgn-gda:DGN569ea0cc293b7f157f1e3acb01f2df2b sio:SIO_000628 miriam-gene:6532, lld:C0029421;
    a sio:SIO_001122 .
}

dgn-np:NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_provenance {
  dgn-np:NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_assertion dcterms:description
      "[To explore the hypothesis that this variability might result from the effects of differing combinations of overlooked variants within SLC6A4 together with small OCD and control sample sizes, we studied three common functional polymorphisms (5-HTTLPR, STin2, and the newly discovered SNP, rs25531) in the largest sample size of OCD patients (N=347) and controls (N=749) ever investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:17375136;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:17+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}